Evidence map›Paper›PMID 28361671›Full record

ArticleBMC genomics2017

Using the entrapment sequence method as a standard to evaluate key steps of proteomics data analysis process.

Xiao-Dong Feng, Li-Wei Li, Jian-Hong Zhang, Yun-Ping Zhu, Cheng Chang, Kun-Xian Shu, Jie Ma

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Xiao-Dong FengChongqing University of Posts and Telecommunications, 2 Chong Wen Road of Nan'an District, Chongqing, 400065, China.
Li-Wei LiDepartment of Bioinformatics, State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Engineering Research Center for Protein Drugs, National Center for Protein Sciences (Beijing), Beijing Institute of Radiation Medicine, 38 Life Science Park Road, Beijing, 102206, China.
Jian-Hong ZhangDepartment of Bioinformatics, State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Engineering Research Center for Protein Drugs, National Center for Protein Sciences (Beijing), Beijing Institute of Radiation Medicine, 38 Life Science Park Road, Beijing, 102206, China.
Yun-Ping ZhuDepartment of Bioinformatics, State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Engineering Research Center for Protein Drugs, National Center for Protein Sciences (Beijing), Beijing Institute of Radiation Medicine, 38 Life Science Park Road, Beijing, 102206, China.
Cheng ChangDepartment of Bioinformatics, State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Engineering Research Center for Protein Drugs, National Center for Protein Sciences (Beijing), Beijing Institute of Radiation Medicine, 38 Life Science Park Road, Beijing, 102206, China.
Kun-Xian ShuChongqing University of Posts and Telecommunications, 2 Chong Wen Road of Nan'an District, Chongqing, 400065, China. shukx@cqupt.edu.cn.
Jie MaDepartment of Bioinformatics, State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Engineering Research Center for Protein Drugs, National Center for Protein Sciences (Beijing), Beijing Institute of Radiation Medicine, 38 Life Science Park Road, Beijing, 102206, China. majie@hupo.org.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe mass spectrometry based technical pipeline has provided a high-throughput, high-sensitivity and high-resolution platform for post-genomic biology. Varied models and algorithms are implemented by different tools to improve proteomics data analysis. The target-decoy searching strategy has become the most popular strategy to control false identification in peptide and protein identifications. While this strategy can estimate the false discovery rate (FDR) within a dataset, it cannot directly evaluate the false positive matches in target identifications.

resultsAs a supplement to target-decoy strategy, the entrapment sequence method was introduced to assess the key steps of mass spectrometry data analysis process, database search engines and quality control methods. Using the entrapment sequences as the standard, we evaluated five database search engines for both the origanal scores and reprocessed scores, as well as four quality control methods in term of quantity and quality aspects. Our results showed that the latest developed search engine MS-GF+ and percolator-embeded quality control method PepDistiller performed best in all tools respectively. Combined with efficient quality control methods, the search engines can improve the low sensitivity of their original scores. Moreover, based on the entrapment sequence method, we proved that filtering the identifications separately could increase the number of identified peptides while improving the confidence level.

conclusionIn this study, we have proved that the entrapment sequence method could be an useful strategy to assess the key steps of the mass spectrometry data analysis process. Its applications can be extended to all steps of the common workflow, such as the protein assembling methods and data integration methods.

Indexed as

Search EngineArchaeal ProteinsDatabases, ProteinDatasets as TopicHumansPeptidesProteomicsPyrococcus furiosusQuality ControlSequence Analysis, ProteinTandem Mass SpectrometryArchaeal ProteinsPeptidesEntrapment sequence methodProteomicsQuality controlTandem mass spectrometryTarget-decoy search

Identifiers

PMID28361671
PMCPMC5374549

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.